
Clinical Research Coordinator
At Novo Nordisk, we are looking for a highly motivated and detail-oriented individual to join our team as a Clinical Research Coordinator. As a global healthcare company committed to improving the lives of millions, we need someone who is passionate about helping us make a difference in the world. If you have a strong background in clinical research and a drive to excel in a fast-paced and dynamic environment, we want to hear from you. Join us in our mission to develop life-changing treatments and make a positive impact on the lives of patients worldwide.
- Conduct and coordinate clinical research studies in compliance with all applicable regulations and protocols.
- Recruit and screen potential participants for clinical trials.
- Coordinate the informed consent process and ensure all necessary documentation is obtained.
- Collect and maintain accurate and complete study data, including patient medical histories and test results.
- Manage study timelines and ensure all activities are completed according to schedule.
- Collaborate with cross-functional teams to ensure study objectives are met.
- Monitor and report adverse events and protocol deviations.
- Assist with the development of study protocols and informed consent forms.
- Ensure all study materials are appropriately stored and maintained.
- Communicate effectively with study participants, healthcare providers, and study sponsors.
- Adhere to ethical and safety standards in all aspects of the study.
- Participate in training and educational opportunities to stay updated on industry and regulatory changes.
- Maintain accurate and organized study documentation.
- Analyze and report study data to support study conclusions.
- Contribute to the development and implementation of new research projects.
- Maintain confidentiality of all study-related information.
- Adhere to Novo Nordisk’s values and code of conduct.
- Assist in the preparation of study reports and presentations.
- Travel to research sites as needed.
- Continuously seek ways to improve study processes and procedures.
Excellent Communication And Interpersonal Skills, With The Ability To Work Effectively With Cross-Functional Teams And External Stakeholders.
Minimum Of A Bachelor's Degree In A Scientific Or Healthcare Field, Such As Biology, Chemistry, Nursing, Or Pharmacy.
At Least 2 Years Of Experience In Clinical Research, Preferably In A Pharmaceutical Or Biotech Company Setting.
Knowledge Of Fda Regulations And Ich Guidelines Related To Clinical Research.
Strong Organizational And Project Management Skills, With The Ability To Prioritize And Manage Multiple Tasks Simultaneously.
Budget management
Quality Control
Report Writing
Data collection
Regulatory compliance
Patient Recruitment
Informed Consent
Protocol Management
Study Coordination
Clinical Assessments
Investigator Meetings
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
flexibility
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Clinical Research Coordinator in London, UK is between £30,000 and £40,000 per year. However, this can vary depending on the specific role, experience, and location within London. Some CRCs may earn higher salaries, up to £50,000 per year or more, especially in more senior or specialized positions. Additionally, salaries may also be influenced by the industry or organization the CRC is working in, as well as any additional benefits or bonuses offered.
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Novo Nordisk AS engages in the research, development, manufacture, and marketing of pharmaceutical products. It operates through the Diabetes and Obesity Care; and Biopharmaceuticals segments. The Diabetes and Obesity Care segment covers insulins, glucagon-like-peptide 1, other protein-related products, oral anti-diabetic drugs and obesity. The Biopharmaceuticals segment handles the research, development, manufacture, and distribution of products within the areas of haemophilia, growth hormone, hormone replacement, inflammation and other therapy areas.

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